He hopes to test samples of martian soil for ancient ribosomal
RNA gene sequences that are conserved in all of Earth's known life forms.
We examined 13,355 prokaryotic ribosomal
RNA gene sequences from multiple colonic mucosal sites and feces of healthy subjects to improve our understanding of gut microbial diversity.
After six to eight weeks, the microbial content of the mice's feces were analyzed by 16S ribosomal
RNA gene sequencing, which showed that approximately 20 kinds of oral bacteria were present in these mice.
In this study, we used ribosomal
RNA gene sequencing to identify the zooxanthellae, bacteria and archaea associated with healthy and yellow band diseased (YBD) colonies in the Media Luna reef of La Parguera, Puerto Rico, in order to examine the influence of YBD on the Montastraea faveolata microbiome.
Not exact matches
Here's why: In the late 90s, technology emerged enabling researchers to rapidly
sequence RNA and DNA — giving them the ability to isolate and record the activity of single
genes.
Citation: Lemay DG, Ballard OA, Hughes MA, Morrow AL, Horseman ND, Nommsen - Rivers LA (2013)
RNA Sequencing of the Human Milk Fat Layer Transcriptome Reveals Distinct
Gene Expression Profiles at Three Stages of Lactation.
In addition, they also used exome
sequencing and RNAseq —
sequencing directly targeted to the SHIP1
gene — to examine the structure of the SHIP1
gene at both the DNA and the
RNA level.
The vaccine can be targeted to the chosen pathogen by using
RNA molecules which share
sequence identity with the pest's
genes and prevents their expression.
«Decoding the genome's cryptic language: New tool to map
RNA - DNA interactions could help researchers translate
gene sequences into functions.»
RNA molecules can attach to particular DNA
sequences to help control how much protein these particular
genes produce within a given time, and within a given cell.
These are
sequences made in the lab from
RNA — the template used to produce the proteins that
genes code for.
Since messenger
RNA is nothing but the imprint of the
gene whose message it is carrying, it is possible to use it to chemically generate the DNA
sequence or
gene it corresponds to.
Each guide
RNA might hit a single
gene or multiple
genes, depending on the particular guide
sequence.
Using
RNA sequencing, the researchers found multiple
genes whose abnormal expression could lead to the high rate of death for cloned embryos, including failure to implant in the uterus and failure to develop a normal placenta.
To more accurately reflect the mechanisms driving oligodendrogliomas, the researchers used
RNA sequencing to study directly, on a single - cell level,
gene expression in samples from six early - stage human tumors.
MicroRNAs are short
RNA sequences that turn
genes on or off.
Using a technique known as single - cell
RNA sequencing, the team explored more than 65,000 individual cells that exist under normal or inflammatory conditions, looking for
genes that were more active in one state or subpopulation versus another.
In germline cells PIWI proteins silence the
RNA from jumping
genes by cutting them in
sequences of ~ 30 nucleotides that will become piRNAs.
The pilot project tested a dozen or so of the most commonly used
gene promoters (regions of DNA that facilitate
gene transcription) and segments of DNA that encode ribosome - binding sites (
sequences of messenger
RNA that control protein translation) to determine whether they behave consistently in different cellular contexts.
Collaboratively, the research team
sequenced the DNA that encodes the
genes as well as the
RNA from the insect at different developmental stages, to identify when different
genes are expressed and in which tissues and organs.
So to reveal their function, biologists used the
sequence information along with a technique called
RNA - mediated interference (RNAi) to temporarily inactivate each of nearly 17,000 of the worm's
genes.
First described in the 1990s — a discovery that led to the 2006 Nobel Prize — RNAi is a process by which organisms suppress the expression of target
genes through the action of small
RNA segments that bind to corresponding
gene sequences.
«Single - nucleus
RNA sequencing, droplet by droplet: DroNc - Seq, technology that merges single - nucleus
RNA sequencing with microfluidics, brings new scale to
gene expression studies in complex tissues.»
By comparing proteomic and
RNA -
sequencing data from people on different exercise programs, the researchers found evidence that exercise encourages the cell to make more
RNA copies of
genes coding for mitochondrial proteins and proteins responsible for muscle growth.
The
gene - editing success appears to be largely due to one procedural change: The researchers introduced the editing system — the enzyme Cas9 and a guide
RNA sequence that helps the editing machinery find its target — at the same time they injected the mutation - laden sperm into a healthy egg in the lab.
RNA sequencing of both single and clustered CTCs from breast cancer patients identified several
genes expressed at elevated levels in CTC clusters, one of which — a protein called plakoglobin — also was overexpressed in the primary tumors of patients with reduced survival.
Our
RNA sequencing analysis of NAFLD - HCC samples revealed squalene epoxidase (SQLE) as the top outlier metabolic
gene overexpressed in NAFLD - HCC patients.
The technique involves designing double - stranded
RNA molecules that match a
sequence in the
RNA produced by the
gene you want to inactivate.
This
sequence always inserts its DNA next to
genes that are «read» by an enzyme called
RNA polymerase III.
Combining this mouse model with the reliable
RNA sequences allowed an efficient inactivation of
genes in primary cells.
In order to locate all
gene switches, the Freiburg research team used modern
sequencing methods to examine the entire genome — DNA, epigenetic markers and
RNA — during the development, maturation and disease of human cardiac muscle cells.
Using next - generation
RNA sequencing and other advanced technologies, the researchers identified a previously unknown
gene involved in betalain synthesis and revealed which biochemical reactions plants use to convert the amino acid tyrosine into betalains.
They also showed that they could block up to five
genes at once by delivering different
RNA sequences.
Microbiota or microbiome structure,
gene expression, and metabolism were assayed by 16S ribosomal
RNA profiling, whole - community shotgun
sequencing,
RNA -
sequencing, and mass spectrometry.
By using
sequences of
RNA that match specific
gene sequences in a pest, RNAi should leave other species unscathed.
In vitro experiments and high - throughput
RNA sequencing revealed that CTCF deletion profoundly altered the B lymphocyte transcriptional program, shifting cells from a
gene expression profile typical of the germinal center to one more similar to that seen in plasma cells.
Technologies such as
RNA sequencing are revealing which
genes are expressed in each individual cell.
By using random series of 30 nucleotides — the building blocks of
RNA and DNA — he thought he could give neurons unique barcodes, linking the barcodes across synapses, then create maps of their connections using high - throughput
gene sequencing technology.
In CRISPR - Cas9
gene editing, a guide
RNA sequence (green) helps Cas9 protein (purple) cut DNA at the correct spot.
First, samples of leaves from these plants are collected for in vitro cultures to isolate the fungi; then the DNA and
RNA of fungi are extracted to
sequence them and, through bioinformatic analysis, the researcher can determine the expression, the presence or absence of
genes in the genomes of a species against each other.
Subsequent
RNA sequencing suggested that digoxin inhibits HIV - 1
gene expression as well as the activation and metabolism of CD4 + T cells.
Surprisingly, they found that although the patterns of
gene expression — as shown by the
RNA sequencing — differed between the hepatocellular carcinomas and the liver cancers with biliary phenotype and depended on the histological type, the overall pattern of mutations in the cells was actually similar between the tumors — of either type — that had emerged in patients who had had infections with either hepatitis C or B, and were different in patients without such infections.
Extensive research has already examined the function of microRNAs, a category of small evolutionarily conserved noncoding
RNAs about 22 to 24 nucleotides in length that target protein - coding
genes in a
sequence - specific manner.
The Rutgers scientists show that the transcription activator protein functions by binding to a specific DNA
sequence preceding the target
gene and making adhesive, Velcro - like interactions with
RNA polymerase that stabilize contacts by
RNA polymerase with adjacent DNA
sequences.
To study
gene expression, they then examined
RNA sequencing data from 25 of the biliary - phenotype cancers and 44 hepatocellular cancers.
These are
sequences produced in the lab from the
RNA that is the intermediate step between
gene and the protein it codes for.
Among the key elements engineers need to get an organism such as E. coli to make a protein from a synthesized
gene are extra
sequences such as promoters (to help the cell make
RNA from DNA) and ribosome binding sites (or RBS, which the cell needs to make proteins from the
RNA).
To develop fluorescent in situ
sequencing, scientists first fix in place thousands of
RNAs — including working copies of
genes called messenger
RNAs — in cells, tissues, organs or embryos.
In this way the team could create a composite image representing the
sequence, and location, of
RNA corresponding to every
gene in the human genome.
The team, headed by OIST's Prof. Alexander Mikheyev of the Ecology and Evolution Unit and Dr. Claire Morandin, post-doctoral scholar at the University of Helsinki, collected queens and workers and
sequenced the transcriptome — the full range of messenger
RNA molecules expressed by an organism — of 16 species of ants to create a co-expression network of 36 sets of
genes, that represent groups of similarly expressed
genes.